At Sun Pharma, we commit to helping you “Create your own sunshine”— by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community.
Are You Ready to Create Your Own Sunshine? As you enter the Sun Pharma world, you’ll find yourself becoming ‘Better every day’ through continuous progress. Exhibit self-drive as you ‘Take charge’ and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we ‘Thrive together’ and support each other’s journeys.”
Job Description
- To work as per cGMP and ensure its compliance as per current guideline and SOPs.
- Responsible to take training before execution of allotted work & maintaining the training file.
- Responsible to follow safety precaution as per laboratory procedure.
- Responsible to escalate any issue / incident to reporting manager for prompt corrective action.
- Responsible for method development studies of API & In process Material.
- Responsible for method Validation studies of API & In process Material.
Responsible for stability studies of API & In process Material.
- Responsible to align with organization goal.
- Responsible to investigation of plant OOS and OOT
- Other responsibilities assigned by reporting authority.
- Responsible to follow Quality Management Document procedure.
- Responsible to perform the calibration of instrument.
- Responsible to prepare Study Protocol and Study Reports.
- Responsible to maintain instrument/equipment as per SOPs.
- Responsible to follow safety precaution as per laboratory procedure.
- Responsible to ensure proper Handling and Disposal of waste.
